ESCCdb: An Integrated Database for Esophageal Squamous Cell Carcinoma
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Consensus DEGs
Recurrent Mutations
Significant CNV
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Somatic mutations of TRIM36:
 
NM_001300752
Mutation details:
6
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NM_001300759
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Mutation details:
8
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mutation records.
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NM_018700
Mutation details:
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NM_001017398
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Mutation details:
3
records
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3
mutation records.
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